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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02361268
Other study ID # 141325
Secondary ID K23AT006965
Status Completed
Phase N/A
First received January 29, 2015
Last updated July 13, 2017
Start date July 2015
Est. completion date May 2017

Study information

Verified date July 2017
Source Vanderbilt University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the effects of intra-dialysis yoga to an educational program among patients with end-stage renal disease. The investigators hypothesize that yoga as compared to the educational program will significantly improve quality of life.


Description:

The investigators propose a prospective, randomized clinical trial among on maintenance hemodialysis to compare the effects of intra-dialysis yoga to an educational program. In a sample of 68 patients the investigators will compare the clinical effects of a 12-week program of yoga to a 12-week education program during dialysis. Outcome assessment of study participants will occur at baseline, 6-weeks, 12-weeks, and 24 weeks for: disease-related quality of life (physical component primary outcome of the study), physical performance, blood pressure, fatigue, satisfaction with dialysis, sleep quality, and mood. Among a sub-sample of 20 participants, the investigators will measure the potential effects of the interventions on endothelial function, arterial stiffness, and autonomic tone. The sub-study will collect outcomes at baseline and 12 weeks.


Recruitment information / eligibility

Status Completed
Enrollment 67
Est. completion date May 2017
Est. primary completion date May 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Maintenance hemodialysis for =3 or months

- Adequately dialyzed (Kt/V =1.2 measured within last 3 months)

- Expected to remain in present hemodialysis shift for next 4 months

- Expected to remain on hemodialysis for at least 6 months

- 18 years or older

Exclusion Criteria:

- Acute or chronic medical conditions that would make intra-dialysis yoga potentially hazardous

- Unstable cardiac disease e.g. angina, life threatening arrhythmia

- Chronic lung disease that prevents gentle exercise or deep breathing exercises

- Active cerebrovascular disease

- Major depression

- Chronic symptoms of nausea, vomiting, or diarrhea

- Current participation in exercise or mind body program/practice

- Cognitive impairment (MME = 24) measured at baseline testing visit

Study Design


Intervention

Behavioral:
Intradialysis-yoga
The experimental intervention in this study is intra-dialysis yoga. The intra-dialysis yoga protocol consists of yoga instruction and practice being offered three times a week for 12 weeks. Subjects will have the opportunity to participate in 15 to 60 minutes of yoga during dialysis.
Educational program
The educational intervention in this study consists of 12 modules of an educational course, Kidney School, developed and maintained by the Medical Education Institute, Inc. Kidney School is a comprehensive, free, educational curriculum for people with kid

Locations

Country Name City State
United States Vanderbilt University Medical Center Nashville Tennessee

Sponsors (2)

Lead Sponsor Collaborator
Vanderbilt University Medical Center National Center for Complementary and Integrative Health (NCCIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in Physical Component Summary of Kidney Disease Quality of Life-36 questionnaire at 6 weeks, 12 weeks, and 24 weeks. The Kidney Disease Quality of Life-36 instrument is a 36-item instrument that contains a generic core (Short Form-12) plus the burden of kidney disease, symptoms/problem of kidney disease, and effects of kidney disease scales. Baseline, 6 weeks, 12 weeks, and 24 weeks
Secondary Functional Assessment of Chronic Illness Therapy-Fatigue Questionnaire to assess fatigue among chronic disease patients Baseline, 6, 12, and 24 weeks
Secondary Profile of Mood States Questionnaire to assess emotional states Baseline, 6, 12, and 24 weeks
Secondary Center for Epidemiological Studies Depression Questionnaire to assess depressive symptoms Baseline, 6, 12, and 24 weeks
Secondary End-stage renal disease: Patient satisfaction Questionnaire to assess patient satisfaction with dialysis treatment Baseline, 6, 12, and 24 weeks
Secondary Pittsburgh Sleep Quality Index Questionnaire to assess sleep quality Baseline, 6, 12, and 24 weeks
Secondary Self-efficacy for self-management Questionnaire to assess self-efficacy for self-management Baseline, 6, 12, and 24 weeks
Secondary 6-minute walk test Assessment of physical performance Baseline, 12, and 24 weeks
Secondary Blood pressure Baseline and weekly over 12 week study period
Secondary Measure of endothelial function with flow-mediated vasodilatation Sub-set of patients will have this assessment of endothelial function which measures percentage change in diameter measured in millimeters Baseline and 12-weeks
Secondary Measure of arterial stiffness from radial artery based pulse wave analysis Sub-set of patient will have this assessment of arterial stiffness as augmentation index Baseline and 12-weeks
Secondary Autonomic tone Assessment of cardiovagal and sympathoneural functioning including baroreflex and heart rate variability Baseline and 12-weeks
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